돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 480343생성일: 2026년 10월 25일

Methyl 5-bromothiophene-2-carboxylate → 5-(3-tert-Butoxycarbonylamino-prop-1-ynyl)-thiophene-2-carboxylic Acid Methyl Ester

https://huagongshe.com/reaction/480343

반응식

참여 물질

역할이름HCID투입량
반응물Methyl 5-bromothiophene-2-carboxylateHCID 605713—
반응물tert-butyl N-(prop-2-yn-1-yl)carbamateHCID 11073648—
촉매TriethylamineHCID 8471—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
용매AcetonitrileHCID 6342—
용매Ethyl AcetateHCID 8857—
생성물5-(3-tert-Butoxycarbonylamino-prop-1-ynyl)-thiophene-2-carboxylic Acid Methyl EsterHCID 5407533963,406.199%

반응 단계

A mixture of prop-2-ynyl-carbamic acid tert-butyl ester (1.67 g, 0.011 mmol), 5-bromo-thiophene-2-carboxylic acid methyl ester (2.50 g, 0.011 mmol), tetrakistriphenylphosphine(0) palladium (0.622 g, 0.0538 mmol), CuI (0.102 g, 0.538 mmol) and triethylamine (1.57 mL, 0.011 mmol) in 50 mL acetonitrile under nitrogen was heated at reflux for 16 h. The reaction was cooled to room temperature, diluted with 75 mL EtOAc, washed with 5.5% HCl, water and brine, dried over MgSO4, filtered and concentrated in vacuo to an oil. The product was purified via flash chromatography (9:1 to 4:1 hexanes:EtOAc) to afford the title compound as an oil (2.06 g). MS 313 (M+18).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06649657B2
출처 데이터셋uspto-grants-2003_11
ORD IDord-6f54f91d847e41e6b7ab1df117abed0c
출처 메모uspto-grants-2003_11